Cleared Traditional

K931917 - SUTURE NON-ABSORBABLE SYNTHETIC POLYPROPYLENE

K931917 is an FDA 510(k) clearance for SUTURE NON-ABSORBABLE SYNTHETIC POLYPRO..., manufactured by Surgimetrics International, Ltd.. The device is a Class 2 General & Plastic Surgery device with product code GAW cleared through the Traditional 510(k) pathway after a 321-day FDA review.

K931917 · Surgimetrics International, Ltd. · General & Plastic Surgery device
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Mar 1994
Decision
321d
Days
Class 2
Risk

K931917 is an FDA 510(k) clearance for the SUTURE NON-ABSORBABLE SYNTHETIC POLYPROPYLENE. Classified as Suture, Nonabsorbable, Synthetic, Polypropylene (product code GAW), Class II - Special Controls.

Submitted by Surgimetrics International, Ltd. (Norcross, US). The FDA issued a Cleared decision on March 3, 1994 after a review of 321 days - an unusually long review period, suggesting complex equivalence evaluation.

This device falls under the General & Plastic Surgery FDA review panel, regulated under 21 CFR 878.5010 - the FDA general and plastic surgery device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Elevated predicate reliance profile. This clearance follows a standard predicate-based equivalence path within the General & Plastic Surgery review framework, consistent with the majority of Class II 510(k) submissions.

View all Surgimetrics International, Ltd. devices

FDA 510(k) Submission Details - K931917

510(k) Number K931917 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 1993
Decision Date March 03, 1994
Days to Decision 321 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
206d slower than avg
Panel avg: 115d · This submission: 321d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

GAW Device Classification - Class 2, Special Controls

Product Code GAW Suture, Nonabsorbable, Synthetic, Polypropylene
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 878.5010
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most General & Plastic Surgery devices follow this clearance model.

Regulatory Peers - GAW Suture, Nonabsorbable, Synthetic, Polypropylene

All 73
Devices cleared under the same product code (GAW) and FDA review panel - the closest regulatory comparables to K931917.
USSC POLYPROPLENE SUTURE
K954808 · United States Surgical, A Division of Tyco Healthc · Feb 1996
PRODEK
K953609 · Sutures , Ltd. · Jan 1996
SURGILENE(R) SUTURES
K945701 · Davis & Geck, Inc. · Jan 1995
REVISED LABELING FOR POLYPROPYLENE SUTURE
K926588 · Look, Inc. · Dec 1993
SURGILENE POLYPROPYLENE SUTURE
K930587 · Davis & Geck, Inc. · Dec 1993
MOPYLEN SUTURE
K931614 · S. Jackson, Inc. · Dec 1993